NP-MRD: Showing NP-Card for 6-hydroxy-14-methoxy-10-oxo-4-pentyl-12-propanoyl-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-5-carboxylic acid (NP0167632)

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Record Information

Version

2.0

Created at

2022-09-03 03:15:39 UTC

Updated at

2022-09-03 03:15:39 UTC

NP-MRD ID

NP0167632

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-hydroxy-14-methoxy-10-oxo-4-pentyl-12-propanoyl-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-5-carboxylic acid

Description

Sublobaric acid, also known as sublobarate, belongs to the class of organic compounds known as depsides and depsidones. These are polycyclic compounds that is either a polyphenolic compound composed of two or more monocyclic aromatic units linked by an ester bond (depside), or a compound containing the depsidone structure (depsidone). 6-hydroxy-14-methoxy-10-oxo-4-pentyl-12-propanoyl-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-5-carboxylic acid is found in Anzia hypoleucoides. Based on a literature review very few articles have been published on Sublobaric acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032205152D          

 31 33  0  0  0  0            999 V2000
    0.2602   -3.1747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9746   -2.7622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6891   -3.1747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4036   -2.7622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1181   -3.1747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8325   -2.7622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5470   -3.1747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2615   -2.7622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2615   -1.9372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5470   -1.5247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5470   -0.6997    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8325   -1.9372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1181   -1.5247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4036   -1.9372    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1181   -0.6997    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0294   -3.0636    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2726   -3.8520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0884   -3.9749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8079   -4.5336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9852   -4.5953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6272   -5.3386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0920   -6.0202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7340   -6.7635    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1987   -7.4452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9147   -5.9586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2726   -5.2153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0953   -5.1536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4533   -4.4103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5600   -5.8353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3827   -5.7736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4240   -3.9905    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
  6 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  2  0  0  0  0
 19 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 20 31  1  0  0  0  0
  7 31  1  0  0  0  0
M  END

     RDKit          3D

 55 57  0  0  0  0  0  0  0  0999 V2000
    5.3402   -0.3358    0.6095 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8689    0.9106    1.2699 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4142    1.1302    1.1911 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7684    1.3268   -0.0796 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6307    0.3845   -1.1934 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9731   -0.9050   -0.9716 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6810   -0.8931   -0.3995 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0273   -2.0704   -0.2020 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6115   -3.2614   -0.5530 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8633   -3.2866   -1.1112 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3924   -4.5267   -1.4411 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5713   -2.0829   -1.3335 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8286   -2.2730   -2.0077 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2095   -3.4434   -2.3408 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7136   -1.2922   -2.3588 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2567   -2.2657    0.3503 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0845   -1.2754    0.8628 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9556   -1.5814    1.7392 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1148    0.1622    0.5342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0040    0.8647    0.1221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1531    2.2132   -0.0922 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3818    2.8439    0.1006 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5224    4.1969   -0.1146 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7150    4.9029    0.0550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4580    2.0914    0.5119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3495    0.7107    0.7407 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5058   -0.0923    1.1027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9672    0.0264    2.2629 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1695   -1.0368    0.1735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2662   -1.8119    0.8720 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2834    0.4314   -0.1234 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9008   -0.0662   -0.3249 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5313   -1.0138    0.3907 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1041   -0.8383    1.2884 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4287    1.8065    0.8566 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2354    0.8907    2.3497 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2294    2.0961    1.8071 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8743    0.3861    1.8702 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8145    1.9862    0.0303 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4193    2.1960   -0.5782 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0712    0.9650   -2.0144 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6227    0.2370   -1.6397 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0700   -4.2054   -0.3844 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9171   -5.3814   -1.2951 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1683   -1.2131   -3.2505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3535    2.8376   -0.4122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4949    5.9828    0.2961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2995    4.8374   -0.9043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3272    4.5437    0.8952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4332    2.5277    0.6752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6557   -0.4413   -0.6818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5196   -1.7422   -0.3490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1870   -1.6810    1.9887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1311   -2.9126    0.7154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2588   -1.5594    0.4950 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7 31  1  0
 31 20  1  0
 20 19  2  0
 19 26  1  0
 26 25  2  0
 25 22  1  0
 22 23  1  0
 23 24  1  0
 22 21  2  0
 26 27  1  0
 27 28  2  0
 27 29  1  0
 29 30  1  0
 19 17  1  0
 17 18  2  0
 17 16  1  0
 16  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 10 12  2  0
 12 13  1  0
 13 15  1  0
 13 14  2  0
 12  6  1  0
  8  7  1  0
 21 20  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  2 36  1  0
  3 37  1  0
  3 38  1  0
  4 39  1  0
  4 40  1  0
  5 41  1  0
  5 42  1  0
 25 50  1  0
 24 47  1  0
 24 48  1  0
 24 49  1  0
 21 46  1  0
 29 51  1  0
 29 52  1  0
 30 53  1  0
 30 54  1  0
 30 55  1  0
  9 43  1  0
 11 44  1  0
 15 45  1  0
M  END


  Mrv1652309032205152D          

 31 33  0  0  0  0            999 V2000
    0.2602   -3.1747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9746   -2.7622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6891   -3.1747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4036   -2.7622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1181   -3.1747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8325   -2.7622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5470   -3.1747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2615   -2.7622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2615   -1.9372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5470   -1.5247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5470   -0.6997    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8325   -1.9372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1181   -1.5247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4036   -1.9372    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1181   -0.6997    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0294   -3.0636    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2726   -3.8520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0884   -3.9749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8079   -4.5336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9852   -4.5953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6272   -5.3386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0920   -6.0202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7340   -6.7635    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1987   -7.4452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9147   -5.9586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2726   -5.2153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0953   -5.1536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4533   -4.4103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5600   -5.8353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3827   -5.7736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4240   -3.9905    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
  6 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  2  0  0  0  0
 19 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 20 31  1  0  0  0  0
  7 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0167632

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCC1=C2OC3=C(C(=CC(OC)=C3)C(=O)CC)C(=O)OC2=CC(O)=C1C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C23H24O8/c1-4-6-7-8-13-19(22(26)27)16(25)11-18-21(13)30-17-10-12(29-3)9-14(15(24)5-2)20(17)23(28)31-18/h9-11,25H,4-8H2,1-3H3,(H,26,27)

> <INCHI_KEY>
CJICVZBHNINYQF-UHFFFAOYSA-N

> <FORMULA>
C23H24O8

> <MOLECULAR_WEIGHT>
428.437

> <EXACT_MASS>
428.147117733

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
44.489935891658334

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6-hydroxy-14-methoxy-10-oxo-4-pentyl-12-propanoyl-2,9-dioxatricyclo[9.4.0.0^{3,8}]pentadeca-1(15),3(8),4,6,11,13-hexaene-5-carboxylic acid

> <ALOGPS_LOGP>
4.18

> <JCHEM_LOGP>
5.357948331333333

> <ALOGPS_LOGS>
-4.25

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.881182576075979

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.5666673050920283

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7521696128685353

> <JCHEM_POLAR_SURFACE_AREA>
119.36

> <JCHEM_REFRACTIVITY>
112.21889999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.41e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-hydroxy-14-methoxy-10-oxo-4-pentyl-12-propanoyl-2,9-dioxatricyclo[9.4.0.0^{3,8}]pentadeca-1(15),3(8),4,6,11,13-hexaene-5-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0       0.486  -5.926   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.819  -5.156   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.153  -5.926   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.487  -5.156   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.820  -5.926   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.154  -5.156   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.488  -5.926   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.821  -5.156   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.821  -3.616   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.488  -2.846   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       8.488  -1.306   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       7.154  -3.616   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.820  -2.846   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.487  -3.616   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       5.820  -1.306   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0      11.255  -5.719   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      11.709  -7.190   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      13.232  -7.420   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      10.841  -8.463   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.306  -8.578   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.637  -9.965   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.505 -11.238   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       8.837 -12.625   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       9.704 -13.898   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.041 -11.123   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.709  -9.735   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      13.245  -9.620   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      13.913  -8.233   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      14.112 -10.892   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      15.648 -10.777   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       8.258  -7.449   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   12                                                  
CONECT    7    6    8   31                                                  
CONECT    8    7    9   16                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10    6   13                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16    8   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   26                                                  
CONECT   20   19   21   31                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22   26                                                       
CONECT   26   25   19   27                                                  
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29                                                            
CONECT   31   20    7                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

View in JSmol

Synonyms

Value	Source
Sublobarate	Generator

Chemical Formula

C₂₃H₂₄O₈

Average Mass

428.4370 Da

Monoisotopic Mass

428.14712 Da

IUPAC Name

6-hydroxy-14-methoxy-10-oxo-4-pentyl-12-propanoyl-2,9-dioxatricyclo[9.4.0.0^{3,8}]pentadeca-1(15),3(8),4,6,11,13-hexaene-5-carboxylic acid

Traditional Name

6-hydroxy-14-methoxy-10-oxo-4-pentyl-12-propanoyl-2,9-dioxatricyclo[9.4.0.0^{3,8}]pentadeca-1(15),3(8),4,6,11,13-hexaene-5-carboxylic acid

CAS Registry Number

Not Available

SMILES

CCCCCC1=C2OC3=C(C(=CC(OC)=C3)C(=O)CC)C(=O)OC2=CC(O)=C1C(O)=O

InChI Identifier

InChI=1S/C23H24O8/c1-4-6-7-8-13-19(22(26)27)16(25)11-18-21(13)30-17-10-12(29-3)9-14(15(24)5-2)20(17)23(28)31-18/h9-11,25H,4-8H2,1-3H3,(H,26,27)

InChI Key

CJICVZBHNINYQF-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Anzia hypoleucoides	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as depsides and depsidones. These are polycyclic compounds that is either a polyphenolic compound composed of two or more monocyclic aromatic units linked by an ester bond (depside), or a compound containing the depsidone structure (depsidone).

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Depsides and depsidones

Sub Class

Not Available

Direct Parent

Depsides and depsidones

Alternative Parents

Substituents

Depsidone
Diaryl ether
Salicylic acid or derivatives
Hydroxybenzoic acid
Anisole
Aryl alkyl ketone
Aryl ketone
1-hydroxy-2-unsubstituted benzenoid
1,4-dioxepine
Alkyl aryl ether
Dioxepine
Benzenoid
Dicarboxylic acid or derivatives
Vinylogous acid
Carboxylic acid ester
Lactone
Ketone
Organoheterocyclic compound
Oxacycle
Carboxylic acid
Carboxylic acid derivative
Ether
Organooxygen compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	4.18	ALOGPS
logP	5.36	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	2.57	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	119.36 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	112.22 m³·mol⁻¹	ChemAxon
Polarizability	44.49 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78435047

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139587758

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6-hydroxy-14-methoxy-10-oxo-4-pentyl-12-propanoyl-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-5-carboxylic acid (NP0167632)

MOL for NP0167632 (6-hydroxy-14-methoxy-10-oxo-4-pentyl-12-propanoyl-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-5-carboxylic acid)

3D MOL for NP0167632 (6-hydroxy-14-methoxy-10-oxo-4-pentyl-12-propanoyl-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-5-carboxylic acid)

3D SDF for NP0167632 (6-hydroxy-14-methoxy-10-oxo-4-pentyl-12-propanoyl-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-5-carboxylic acid)

3D-SDF for NP0167632 (6-hydroxy-14-methoxy-10-oxo-4-pentyl-12-propanoyl-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-5-carboxylic acid)

PDB for NP0167632 (6-hydroxy-14-methoxy-10-oxo-4-pentyl-12-propanoyl-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-5-carboxylic acid)

3D PDB for NP0167632 (6-hydroxy-14-methoxy-10-oxo-4-pentyl-12-propanoyl-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-5-carboxylic acid)

SMILES for NP0167632 (6-hydroxy-14-methoxy-10-oxo-4-pentyl-12-propanoyl-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-5-carboxylic acid)

INCHI for NP0167632 (6-hydroxy-14-methoxy-10-oxo-4-pentyl-12-propanoyl-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-5-carboxylic acid)

Structure for NP0167632 (6-hydroxy-14-methoxy-10-oxo-4-pentyl-12-propanoyl-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-5-carboxylic acid)

3D Structure for NP0167632 (6-hydroxy-14-methoxy-10-oxo-4-pentyl-12-propanoyl-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-5-carboxylic acid)